FDA Inspection
Rebuilder Medical, Inc.Rebuilder Medical, Inc. – FDA Inspection, Aug 17, 2009
Record Details
This FDA Inspection record concerns Rebuilder Medical, Inc., with an inspection on August 17, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Rebuilder Medical, Inc.
- Inspection Date
- August 17, 2009
- Product Type
- Devices
View Company Profile
ID · 4b0372f9-a95c-4e3e-816d-112f87b8f686
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 604183
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.198(a)General
- 21 CFR 820.198(a)Complete files maintained
- 21 CFR 820.80(d)(3)No release signature
- 21 CFR 820.181(b)DMR production process specifications
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Other FDA inspections of Rebuilder Medical, Inc.
8| Date | Classification | Office | Project area |
|---|---|---|---|
| November 29, 2022 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 21, 2022 | NAI | Center for Food Safety and Applied Nutrition | Foodborne Biological Hazards |
| August 21, 2019 | NAI | Center for Food Safety and Applied Nutrition | Food Composition, Standards, Labeling and Econ |
| August 22, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 20, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Rebuilder Medical, Inc.
- FDA Inspection 1191631 - 2022-11-29
- FDA Inspection 1172533 - 2022-06-21
- FDA Inspection 1109897 - 2019-08-21
- FDA Inspection 1063183 - 2018-08-22
- FDA Inspection 900259 - 2014-10-20
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